15302-18-8

Basic information

• Product Name: Formetorex
• Synonyms: Formetorex;formetamide;N-(1-Methyl-2-phenylethyl)formamide;N-(α-Methylphenethyl)formamide;N-Formyl-1-phenyl-2-propaneamine
• CAS NO: 15302-18-8
• Molecular Weight: 0
• Mol File: 15302-18-8.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 336.9°C at 760 mmHg
• Flash Point: 197.9°C
• Appearance: /
• Density: 1.008g/cm³
• Vapor Pressure: 0.000108mmHg at 25°C
• Refractive Index: 1.515
• CAS DataBase Reference: Formetorex(CAS DataBase Reference)
• NIST Chemistry Reference: Formetorex(15302-18-8)
• EPA Substance Registry System: Formetorex(15302-18-8)

Safety Data

• Hazardous Substances Data: 15302-18-8(Hazardous Substances Data)

Usage

General Description

Formetorex is a stimulant drug that is chemically similar to amphetamine and methamphetamine. It acts as a releasing agent of norepinephrine and dopamine in the brain, leading to increased energy, alertness, and euphoria. Formetorex has also been found to have appetite-suppressing effects, making it popular for use as a weight-loss aid. However, due to its similarities to other illicit stimulants, Formetorex is considered a controlled substance and is illegal to possess and distribute in many countries. Its use carries a risk of addiction, abuse, and negative health consequences, including heightened blood pressure, heart rate, and potential cardiovascular issues.

InChI:InChI=1/C10H13NO/c1-9(11-8-12)7-10-5-3-2-4-6-10/h2-6,8-9H,7H2,1H3,(H,11,12)/t9-/m1/s1

Upstream product

• 51-64-9 dexamfetamine 
• 109-94-4 formic acid ethyl ester 
• 60-15-1 2-amino-1-phenylpropane 
• 41820-21-7 (-)-Amphetamine hydrochloride 
• 214679-11-5 (1R,2S,1'S)-(+)-N-<2-(1'-tert-butoxycarbonylaminomethyl-2'-methylpropoxy)-1-methyl-2-phenylethyl>formamide 
• 68-12-2 N,N-dimethyl-formamide 
• 123-39-7 N-Methylformamide 
• 103-79-7 1-phenyl-acetone 
• 7677-24-9 trimethylsilyl cyanide 
• 698-87-3 3-phenyl-2-propanol 
• 64-18-6 formic acid 
• 77287-34-4 formamide 
• 214679-09-1 (1S,2R,1'R,2'S)-(-)-N-<1-methyl-2-(2'-nitrocyclohexyloxy)-2-phenylethyl>formamide 
• 214678-95-2 (1S,2R,1'R)-(-)-N-<1-methyl-2-(1'-nitromethylbutoxy)-2-phenylethyl>formamide 

Downstream Products

• 15547-41-8 (R)-3-methyl-3,4-dihydroisoquinoline 
• 14123-78-5 3-methyl-3,4-dihydro-isoquinoline 

Relevant articles and documents

Method for synthesizing formamide derivatives by molybdenum catalyzed formylation reaction

The invention discloses a method for synthesizing formamide derivatives by molybdenum catalyzed formylation reaction. The method includes that the formamide derivatives are generated by one-pot reaction of amine compounds and formamide compounds under the catalytic action of molybdenum salts and/or molybdenum oxides. Reaction methods and catalysts are cheap and easy to acquire, reaction steps andoperations are simple, the method has advantages of high reaction selectivity, high yield, expandability in reaction and the like, and defects of high toxicity of reaction agents, expensive catalysts,complex reaction steps, high quality of by-products and the like in the prior art are overcome.

Method of using graphene oxide to catalyze formylation reaction to synthesize formamide derivative

The invention discloses a method of using graphene oxide to catalyze formylation reaction to synthesize a formamide derivative. The method includes: allowing amine compound and formamide compound to be in one-pot reaction under catalytic action of graphene oxide to generate the formamide derivative. Reaction raw materials and a catalyst are low in cost and easy to obtain, the catalyst can be recycled, reaction steps and operations are simple, the method has the advantages of high reaction selectivity, high yield and supportiveness of expanding reaction, and the defects that reaction reagents are high in toxicity, catalysts are expensive, the number of reaction steps is large and the number of byproducts is large in the prior art are overcome.

Efficient isocyanide-less isocyanide-based multicomponent reactions

Isocyanides are the Jekyll and Hyde of organic chemistry allowing for extremely interesting transformations that are not only extremely odorous but also noxious. Therefore, an isocyanide-less isocyanide-based multicomponent reaction (IMCR) has been developed, and this protocol is expected to replace many of the old procedures in the future not only in IMCR but in other areas of organic chemistry as well.